These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

249 related articles for article (PubMed ID: 17611575)

  • 1. Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families.
    Leter EM; Koopmans AK; Gille JJ; van Os TA; Vittoz GG; David EF; Jaspars EH; Postmus PE; van Moorselaar RJ; Craanen ME; Starink TM; Menko FH
    J Invest Dermatol; 2008 Jan; 128(1):45-9. PubMed ID: 17611575
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer.
    Nahorski MS; Lim DH; Martin L; Gille JJ; McKay K; Rehal PK; Ploeger HM; van Steensel M; Tomlinson IP; Latif F; Menko FH; Maher ER
    J Med Genet; 2010 Jun; 47(6):385-90. PubMed ID: 20522427
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families.
    Houweling AC; Gijezen LM; Jonker MA; van Doorn MB; Oldenburg RA; van Spaendonck-Zwarts KY; Leter EM; van Os TA; van Grieken NC; Jaspars EH; de Jong MM; Bongers EM; Johannesma PC; Postmus PE; van Moorselaar RJ; van Waesberghe JH; Starink TM; van Steensel MA; Gille JJ; Menko FH
    Br J Cancer; 2011 Dec; 105(12):1912-9. PubMed ID: 22146830
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial multiple discoid fibromas: a look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus.
    Starink TM; Houweling AC; van Doorn MB; Leter EM; Jaspars EH; van Moorselaar RJ; Postmus PE; Johannesma PC; van Waesberghe JH; Ploeger MH; Kramer MT; Gille JJ; Waisfisz Q; Menko FH
    J Am Acad Dermatol; 2012 Feb; 66(2):259.e1-9. PubMed ID: 21794948
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of the Birt Hogg Dube gene in patients with multiple lung cysts and recurrent pneumothorax.
    Gunji Y; Akiyoshi T; Sato T; Kurihara M; Tominaga S; Takahashi K; Seyama K
    J Med Genet; 2007 Sep; 44(9):588-93. PubMed ID: 17496196
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Birt-Hogg-Dubé syndrome: clinical and genetic studies of 10 French families.
    Kluger N; Giraud S; Coupier I; Avril MF; Dereure O; Guillot B; Richard S; Bessis D
    Br J Dermatol; 2010 Mar; 162(3):527-37. PubMed ID: 19785621
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Spontaneous pneumothorax as the first manifestation of a hereditary condition with an increased renal cancer risk].
    Johannesma PC; Lammers JW; van Moorselaar RJ; Starink TM; Postmus PE; Menko FH
    Ned Tijdschr Geneeskd; 2009; 153():A581. PubMed ID: 19857281
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Birt-Hogg-Dubé syndrome: diagnosis and management.
    Menko FH; van Steensel MA; Giraud S; Friis-Hansen L; Richard S; Ungari S; Nordenskjöld M; Hansen TV; Solly J; Maher ER;
    Lancet Oncol; 2009 Dec; 10(12):1199-206. PubMed ID: 19959076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Birt-Hogg-Dubé Syndrome: A Review of Dermatological Manifestations and Other Symptoms.
    Tong Y; Schneider JA; Coda AB; Hata TR; Cohen PR
    Am J Clin Dermatol; 2018 Feb; 19(1):87-101. PubMed ID: 28695430
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Birt-Hogg-Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas.
    Näf E; Laubscher D; Hopfer H; Streit M; Matyas G
    Fam Cancer; 2016 Jan; 15(1):127-32. PubMed ID: 26342594
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Case Report of Birt-Hogg-Dubé Syndrome: Germline Mutations of FLCN Detected in Patients With Renal Cancer and Thyroid Cancer.
    Dong L; Gao M; Hao WJ; Zheng XQ; Li YG; Li XL; Yu Y
    Medicine (Baltimore); 2016 May; 95(22):e3695. PubMed ID: 27258496
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distinctive expression patterns of glycoprotein non-metastatic B and folliculin in renal tumors in patients with Birt-Hogg-Dubé syndrome.
    Furuya M; Hong SB; Tanaka R; Kuroda N; Nagashima Y; Nagahama K; Suyama T; Yao M; Nakatani Y
    Cancer Sci; 2015 Mar; 106(3):315-23. PubMed ID: 25594584
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.
    Lim DH; Rehal PK; Nahorski MS; Macdonald F; Claessens T; Van Geel M; Gijezen L; Gille JJ; Giraud S; Richard S; van Steensel M; Menko FH; Maher ER
    Hum Mutat; 2010 Jan; 31(1):E1043-51. PubMed ID: 19802896
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Birt-Hogg-Dubé syndrome: a large single family cohort.
    Skolnik K; Tsai WH; Dornan K; Perrier R; Burrowes PW; Davidson WJ
    Respir Res; 2016 Feb; 17():22. PubMed ID: 26928018
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Birt-Hogg-Dubé syndrome].
    Rehfeld A; van Steensel MA; Friis-Hansen L
    Ugeskr Laeger; 2010 Jul; 172(29):2085-90. PubMed ID: 20633341
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome.
    Schmidt LS; Nickerson ML; Warren MB; Glenn GM; Toro JR; Merino MJ; Turner ML; Choyke PL; Sharma N; Peterson J; Morrison P; Maher ER; Walther MM; Zbar B; Linehan WM
    Am J Hum Genet; 2005 Jun; 76(6):1023-33. PubMed ID: 15852235
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.
    Kayhan G; Yılmaz Demirci N; Turktas H; Ergun MA
    Genet Test Mol Biomarkers; 2017 Oct; 21(10):632-634. PubMed ID: 28805452
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome.
    Furuya M; Yao M; Tanaka R; Nagashima Y; Kuroda N; Hasumi H; Baba M; Matsushima J; Nomura F; Nakatani Y
    Clin Genet; 2016 Nov; 90(5):403-412. PubMed ID: 27220747
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Multiple spontaneous pneumothoraces revealing Birt-Hogg-Dube syndrome].
    Van Denhove A; Guillot-Pouget I; Giraud S; Isaac S; Freymond N; Calender A; Pacheco Y; Devouassoux G
    Rev Mal Respir; 2011 Mar; 28(3):355-9. PubMed ID: 21482341
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants.
    Liu K; Xu W; Tian X; Xiao M; Zhao X; Zhang Q; Qu T; Song J; Liu Y; Xu KF; Zhang X
    Orphanet J Rare Dis; 2019 Oct; 14(1):223. PubMed ID: 31615547
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.